"68788-7056-3" National Drug Code (NDC)

Lovastatin 30 TABLET in 1 BOTTLE (68788-7056-3)
(Preferred Pharmaceuticals Inc.)

NDC Code68788-7056-3
Package Description30 TABLET in 1 BOTTLE (68788-7056-3)
Product NDC68788-7056
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameLovastatin
Non-Proprietary NameLovastatin
Dosage FormTABLET
UsageORAL
Start Marketing Date20180105
Marketing Category NameANDA
Application NumberANDA075991
ManufacturerPreferred Pharmaceuticals Inc.
Substance NameLOVASTATIN
Strength10
Strength Unitmg/1
Pharmacy ClassesHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]

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